EP0726248B1 - Verfahren zur Herstellung von O-Acyloxycarbonsäureaniliden - Google Patents

Verfahren zur Herstellung von O-Acyloxycarbonsäureaniliden Download PDF

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Publication number
EP0726248B1
EP0726248B1 EP96100858A EP96100858A EP0726248B1 EP 0726248 B1 EP0726248 B1 EP 0726248B1 EP 96100858 A EP96100858 A EP 96100858A EP 96100858 A EP96100858 A EP 96100858A EP 0726248 B1 EP0726248 B1 EP 0726248B1
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EP
European Patent Office
Prior art keywords
carbon atoms
employed
hydrogen
radical
alkali metal
Prior art date
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EP96100858A
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German (de)
English (en)
French (fr)
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EP0726248A1 (de
Inventor
Andreas Dr. Dierdorf
Theodor Dr. Papenfuhs
Siegfried Dr. Planker
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Clariant Produkte Deutschland GmbH
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Clariant GmbH
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Publication date
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00—Preparation of carboxylic acid amides
    • C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C235/16—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring

Definitions

  • the present invention relates to a state of the art improved process for the preparation of O-acyloxycarboxylic acid anilides.
  • O-Acyloxycarbonkladilide especially acetoxyacetic anilides interesting precursors for the production of glycolic acid anilides.
  • Glycolic acid anilides in turn are found as important starting materials in both Production of herbicides (EP-A-300 344) and active pharmaceutical ingredients (EP-A-284 338, EP-A-363 284) as well as in the production of fungicides (US 4,440,780) application.
  • DE-OS 30 38 598 describes a process for the production of ⁇ -Hydroxycarboxamides by transesterification of acetoxycarboxamides by means of alcohols in the presence of catalytic amounts of an alkali or Alkaline earth metal hydroxide or carbonate. You set the appropriate ones ⁇ -halocarboxamides with an alkali or alkaline earth acetate in the presence a quaternary ammonium salt and optionally using a Diluent to give the corresponding ⁇ -acetoxycarboxamides, which are then implemented.
  • US 4,334,073 relates to a process for the preparation of ⁇ -hydroxycarboxamides, initially an ⁇ -halocarboxamide with a Alkali acetate or alkaline earth acetate in the presence of a quaternary ammonium salt and a solvent is reacted and then the obtained ⁇ -acetoxycarboxamide to the corresponding ⁇ -hydroxycarboxamide is decarboxylated.
  • O-acyloxycarboxylic acid anilides in particular Acetoxyacetic anilides
  • a method of manufacture of O-Acyloxycarbonklaaniliden provide, on the one hand, the disadvantages avoids the above-mentioned procedures, on the other hand, simple Carry out wisely and using easily accessible starting materials lets and also the desired O-Acyloxycarbonklareanilide both in good Yield and high purity.
  • O-acyloxycarboxylic acid anilides of the general formula (I) in which R represents hydrogen or a radical having 1 to 6 carbon atoms, n is an integer from 1 to 10, R 1 represents hydrogen or an alkyl radical having 1 to 12 carbon atoms, R 2 and R 3 are identical or different and represent hydrogen, an alkyl radical with 1 to 12 carbon atoms, an aryl radical with 6 to 12 carbon atoms, a cycloalkyl radical with 5 to 12 carbon atoms in the ring, an alkenyl or alkynyl radical with 3 to 12 carbon atoms, are NO 2 , F, Cl, Br or CN.
  • R represents hydrogen or a radical having 1 to 6 carbon atoms
  • n is an integer from 1 to 10
  • R 1 represents hydrogen or an alkyl radical having 1 to 12 carbon atoms
  • R 2 and R 3 are identical or different and represent hydrogen, an alkyl radical with 1 to 12 carbon atoms, an aryl radical with 6 to 12 carbon atoms
  • the method according to the invention has several advantages. For one thing it is not limited to the production of acetoxyacetic anilides, but is generally suitable for the production of O-acyloxycarboxylic acid anilides corresponding to the reaction of the chlorocarboxanilide of the formula (II) with the Alkali metal carboxylate of formula (III). On the other hand, it is the Alkali metal carboxylate, the inert solvent as well as in the Carboxylic acid to easily accessible starting materials, which are also used in technical Quantities can be made available. The procedure can be broken down simple way, so without a lot of technical effort, and realize it leads to good yields with high sales. The desired end product is obtained in very high purity.
  • chlorocarboxylic anilides can be of the formula (II), in which n is an integer from 1 to 4, in particular 1 to 2, preferably stands for 1, used with good success.
  • chlorocarboxanilides of the formula (II) in which R 1 is hydrogen or an alkyl radical having 1 to 4 carbon atoms and those in which R 2 and R 3 are identical or different and are hydrogen, an alkyl radical having 1 to 4 carbon atoms for NO 2 , F, Cl, Br or CN and in particular R 2 is hydrogen and R 3 is an alkyl radical having 1 to 4 carbon atoms, NO 2 , F, Cl, Br or CN.
  • alkali metal carboxylates can be used in the process deploy.
  • the chlorocarboxylic acid anilide and the alkali metal carboxylate can be combined in one bring wide molar ratio to the implementation. This is usually used Chlorcarbonklareanilid and the alkali metal carboxylate in a molar ratio of 1: 1 to 1: 5, in particular 1: 1 to 1: 2.
  • Aromatic or aliphatic are suitable as inert solvents Hydrocarbons, for example toluene, o-xylene, m-xylene, p-xylene, mixtures isomeric xylenes, ethylbenzene, mesitylene, chlorobenzene, dichlorobenzene, chlorotoluene, Cyclohexane, cumene, decalin or mixtures of these solvents, in particular Mixtures of more isomeric xylenes and mesitylene.
  • Hydrocarbons for example toluene, o-xylene, m-xylene, p-xylene, mixtures isomeric xylenes, ethylbenzene, mesitylene, chlorobenzene, dichlorobenzene, chlorotoluene, Cyclohexane, cumene, decalin or mixtures of these solvents, in particular Mixtures of more isomeric xylenes and me
  • the alkali metal carboxylate and the carboxylic acid are usually used in a molar ratio of 1: 0.5 to 1: 5, in particular 1: 0.7 to 1: 2.
  • a molar ratio of 1: 0.5 to 1: 5, in particular 1: 0.7 to 1: 2.
  • the resulting alkali metal chloride is after the completion of Reaction, for example by filtration and / or extraction, for example in Form of an aqueous solution, separated.
  • the inert can Separate the solvent by distillation and, if necessary, together with separated carboxylic acid, reinstall in the reaction.
  • Example 2a Yield (%)
  • Example 2b Yield (%) 1 32 32 2nd 54 54 3rd 66 65 4th 75 75 5 83 82 6 87 83 7 89 84 8th 91 86 9 91 86
  • Example 4 The procedure is as given in Example 4, but no glacial acetic acid is added. The course of the reaction is monitored by means of gas chromatographic analysis. The results are shown in Table 5 below. Response time (hours) Comparative Example 3 Yield (%) Example 4 Yield (%) 1 1 37 2nd 2nd 60 3rd 3rd 72 4th 4th 82 5 5 87 6 6 91 7 7 93 8th 8th 95 9 9 98
  • Example 5 The procedure is as indicated in Example 5, but no propionic acid is added. The results are shown in Table 6 below. Response time (hours) Comparative Example 5 Yield (%) Example 5 Yield (%) 1 17th 94 2nd 28 97 3rd 37 98 4th 45 98 5 53 98 6 59 98 7 64 98 8th 68 98 9 72 98 10th 76 98

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP96100858A 1995-02-09 1996-01-23 Verfahren zur Herstellung von O-Acyloxycarbonsäureaniliden Expired - Lifetime EP0726248B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19504225A DE19504225A1 (de) 1995-02-09 1995-02-09 Verfahren zur Herstellung von O-Acyloxycarbonsäureaniliden
DE19504225 1995-02-09

Publications (2)

Publication Number Publication Date
EP0726248A1 EP0726248A1 (de) 1996-08-14
EP0726248B1 true EP0726248B1 (de) 1998-04-15

Family

ID=7753519

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96100858A Expired - Lifetime EP0726248B1 (de) 1995-02-09 1996-01-23 Verfahren zur Herstellung von O-Acyloxycarbonsäureaniliden

Country Status (4)

Country Link
US (1) US5693852A (ja)
EP (1) EP0726248B1 (ja)
JP (1) JPH08245535A (ja)
DE (2) DE19504225A1 (ja)

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE794013A (fr) * 1972-01-13 1973-07-12 Basf Ag Anilides d'acide o-(aminosulfonyl)-glycolique substitues
DE2904490A1 (de) * 1979-02-07 1980-08-21 Bayer Ag Verfahren zur herstellung von alpha -hydroxycarbonsaeureamiden
US4440780A (en) 1979-06-01 1984-04-03 Chevron Research Company Fungicidal 3-(N-acyl-N-arylamino)-and 3-(N-thionoacyl-N-arylamino)-gamma-butyrolactones and gamma-thiobutyrolactones
DE3038598A1 (de) 1980-10-13 1982-05-19 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von (alpha)-hydroxy-carbonsaeureamiden, neue zwischenprodukte hierfuer und verfahren zu deren herstellung
GB8707053D0 (en) 1987-03-25 1987-04-29 Ici Plc Anti-tumour agents
EP0300344B1 (de) 1987-07-23 1993-10-06 Bayer Ag Halogenierte Thiadiazolyl-oxyessig-säureamide, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung als Herbizide
ZA897515B (en) 1988-10-07 1990-06-27 Merrell Dow Pharma Novel peptidase inhibitors

Also Published As

Publication number Publication date
JPH08245535A (ja) 1996-09-24
US5693852A (en) 1997-12-02
DE59600147D1 (de) 1998-05-20
DE19504225A1 (de) 1996-08-14
EP0726248A1 (de) 1996-08-14

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